A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156878



Internal ID22087279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20306406..20488673hg38UCSC Ensembl
Outerchr8:20296439..20492188hg38UCSC Ensembl
Innerchr8:20163917..20346184hg19UCSC Ensembl
Outerchr8:20153950..20349699hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38195750
hg19195750
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020970, nssv4020971
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156878
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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